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A family of mixed-metal cyanide cubes with alternating octahedral and tetrahedral corners exhibiting a variety of magnetic behaviors including single molecule magnetism.

作者信息

Schelter Eric J, Karadas Ferdi, Avendano Carolina, Prosvirin Andrey V, Wernsdorfer Wolfgang, Dunbar Kim R

机构信息

Department of Chemistry, Texas A&M University, College Station, TX 77842-3012, USA.

出版信息

J Am Chem Soc. 2007 Jul 4;129(26):8139-49. doi: 10.1021/ja0683281. Epub 2007 Jun 12.

DOI:10.1021/ja0683281
PMID:17564438
Abstract

A series of structurally related pseudocubic metal cyanide clusters of Re(II) and 3d metal ions [{MX}4{Re(triphos)(CN)3}4] (M = Mn, Fe, Co, Ni, Zn; X = Cl, I, -OCH3) have been prepared, and their magnetic and electrochemical properties have been probed to evaluate the effect of changing the identity of the 3d metal ion. Electrochemistry of the clusters reveals several rhenium-based oxidation and reduction processes, some of which result in cluster fragmentation. The richest electrochemistry was observed for the iron congener, which exists as the Re(I)/Fe(III) cluster at the resting potential and exhibits six clear one-electron reversible redox couples and two, closely spaced one-electron quasi-reversible processes. The [{MnIICl}4{ReII(triphos)(CN)3}4] complex exhibits single molecule magnetism with a fast tunneling relaxation process observed at H = 0 determined by micro-SQUID magnetization measurements. A comparative evaluation of the magnetic properties across the series reveals that the compounds exhibit antiferromagnetic coupling between the metal ions, except for [{NiIICl}4{ReII(triphos)(CN)3}4] that shows ferromagnetic behavior. Despite the large ground-state spin value of [{NiIICl}4{ReII(triphos)(CN)3}4] (S = 6), only manganese congeners exhibit SMM behavior to 1.8 K.

摘要

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